The pharmaceutical dissolution tester is an instrument for measuring the dissolution degree of medicine. It replaces the previous disintegration time limit inspection with scientific and advanced measurement methods, thereby improving the scientific nature of medicine quality control methods and ensuring the clinical efficacy.

Precautions for the operation of dissolution tester to measure tablet dissolution:

1. Check the dissolution tester used in advance whether it operates normally, and check whether the temperature control, speed, etc. are accurate, whether the lifting paddle is flexible.

2. The height of the paddle has a certain influence on the dissolution test. It should be installed at the specified height, and the bottom of the basket (or paddle) should be 25mm away from the bottom of the dissolution cup.

3. Be very careful when changing the release medium, and do not pour out the tablets.

4. After completing a test, rinse the basket, beaker, etc. with normal water and distilled water in turn, and dry them for use. After each sample is measured, this operation should be repeated before measuring another sample.

The dissolution apparatus consists of cabinet, control system, electrical system, water bath system, transmission system, sensors, paddle components, rotating basket components and other components. It has the characteristics of high automation, high control accuracy, high sensitivity, small error, low noise and easy operation.